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IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET

K123987 Class II Traditional
Decision Date
2013-08-27
Sponsor / Applicant
Innovative Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K123987
Product Code JKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 2013-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET received FDA 510(k) clearance under submission number K123987, sponsored by Innovative Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2013-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.